LCMS Scientist for Bioanalysis
- Research & Development
- Denmark - Måløv
The Development Bioanalysis Department is seeking a highly qualified and motivated LCMS scientist to support the diabetes projects. We are developing, validating and using LC-MS/MS bioanalytical methods for quantitative measurement of drugs and excipients in samples from non-clinical and clinical studies.
About the department
The department is responsible for bioanalysis for non-clinical and clinical safety and efficacy evaluations across the entire project portfolio at Novo Nordisk A/S. We are working in a GLP regulated environment and we use WatsonLIMS for collection of data and reporting. The department is part of the Diabetes Research Unit of Novo Nordisk A/S, and is located in Maaloev.
The job
Your main focus will be to develop and validate drug specific LC-MS/MS bioanalytical methods according to current guidelines and analysis of non-clinical and clinical study samples. You will represent the Development Bioanalysis Department in cross functional project teams and be responsible for collaboration and timely delivery of bioanalytical data to stakeholders. You will be responsible for both in-house analyses and analyses at Contract Research Organisations (CRO’s). The latter involves support to the CRO by reviewing their reports and eventually visiting them for troubleshooting and/or reviewing raw data. You will be working with LC-MS/MS equipment from AB Sciex.
Qualifications
You hold a life science academic PhD degree and have a minimum of 3 years experience with development and validation of LC-MS/MS bioanalytical methods and you have preferably experience with automation of the assays. Knowledge of immuno precipitation of peptides/proteins and/or subsequent tryptic digestion will be beneficial. Preferably, you are familiar with EMA/FDA/OECD guidelines and have a quality mindset. Flair for use of IT-systems, and qualification of analytical equipment and software, according to guidelines will be appreciated. You have strong written and oral communication skills in English as well as the capability to work in an interdisciplinary environment.
Experience with managing technicians is an advantage.
You are flexible, ambitious, focused on results and have a good sense of humour. You are good at communicating and collaborating in teams. You will join a team in a highly dynamic and challenging environment within the Development Bioanalysis Department.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Sune Hove Sporring at +45 3079 4905 or Michael Pilgård Andersen at+45 3075 4819 or Lotte Halling at +45 3053 7029.
Deadline
9 January 2014
- Research & Development
- Denmark - Måløv
The Development Bioanalysis Department is seeking a highly qualified and motivated LCMS scientist to support the diabetes projects. We are developing, validating and using LC-MS/MS bioanalytical methods for quantitative measurement of drugs and excipients in samples from non-clinical and clinical studies.
About the department
The department is responsible for bioanalysis for non-clinical and clinical safety and efficacy evaluations across the entire project portfolio at Novo Nordisk A/S. We are working in a GLP regulated environment and we use WatsonLIMS for collection of data and reporting. The department is part of the Diabetes Research Unit of Novo Nordisk A/S, and is located in Maaloev.
The job
Your main focus will be to develop and validate drug specific LC-MS/MS bioanalytical methods according to current guidelines and analysis of non-clinical and clinical study samples. You will represent the Development Bioanalysis Department in cross functional project teams and be responsible for collaboration and timely delivery of bioanalytical data to stakeholders. You will be responsible for both in-house analyses and analyses at Contract Research Organisations (CRO’s). The latter involves support to the CRO by reviewing their reports and eventually visiting them for troubleshooting and/or reviewing raw data. You will be working with LC-MS/MS equipment from AB Sciex.
Qualifications
You hold a life science academic PhD degree and have a minimum of 3 years experience with development and validation of LC-MS/MS bioanalytical methods and you have preferably experience with automation of the assays. Knowledge of immuno precipitation of peptides/proteins and/or subsequent tryptic digestion will be beneficial. Preferably, you are familiar with EMA/FDA/OECD guidelines and have a quality mindset. Flair for use of IT-systems, and qualification of analytical equipment and software, according to guidelines will be appreciated. You have strong written and oral communication skills in English as well as the capability to work in an interdisciplinary environment.
Experience with managing technicians is an advantage.
You are flexible, ambitious, focused on results and have a good sense of humour. You are good at communicating and collaborating in teams. You will join a team in a highly dynamic and challenging environment within the Development Bioanalysis Department.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Sune Hove Sporring at +45 3079 4905 or Michael Pilgård Andersen at+45 3075 4819 or Lotte Halling at +45 3053 7029.
Deadline
9 January 2014